CSNK2A1, casein kinase 2 alpha 1, 1457

N. diseases: 87; N. variants: 11
Disease: Dysmorphic features ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs869312845
rs869312845
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C0432072
Disease:
Dysmorphic features 		T 0.700 GeneticVariation CLINVAR Okur-Chung neurodevelopmental syndrome: Eight additional cases with implications on phenotype and genotype expansion. 29240241 2018
dbSNP: rs869312845
rs869312845
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C0432072
Disease:
Dysmorphic features 		T 0.700 GeneticVariation CLINVAR Prevalence and architecture of de novo mutations in developmental disorders. 28135719 2017
dbSNP: rs869312845
rs869312845
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C0432072
Disease:
Dysmorphic features 		T 0.700 GeneticVariation CLINVAR De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features. 27048600 2016
dbSNP: rs869312845
rs869312845
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C0432072
Disease:
Dysmorphic features 		T 0.700 GeneticVariation CLINVAR Presynaptic CK2 promotes synapse organization and stability by targeting Ankyrin2. 24395637 2014
dbSNP: rs869312845
rs869312845
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C0432072
Disease:
Dysmorphic features 		T 0.700 GeneticVariation CLINVAR Predominance of CK2α over CK2α' in the mammalian brain. 21761202 2011
dbSNP: rs869312845
rs869312845
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C0432072
Disease:
Dysmorphic features 		T 0.700 GeneticVariation CLINVAR The alpha catalytic subunit of protein kinase CK2 is required for mouse embryonic development. 17954558 2008